Dicyclomine Hydrochloride
- Product NDC
- 63629-6820
- 11-digit product format
- 636296820
- Labeler code
- 63629
- Product ID
- 63629-6820_e56f5f42-b058-4aa9-858d-c5a8ba56f6d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA085223
- Marketing category
- ANDA
- Marketing start
- 1986-07-30
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6820-1 | 63629682001 | 30 TABLET in 1 BOTTLE (63629-6820-1) | 30 tablet | 2015-10-15 | 0000-00-00 | No | No | Current |
| 63629-6820-2 | 63629682002 | 60 TABLET in 1 BOTTLE (63629-6820-2) | 60 tablet | 2015-10-15 | 0000-00-00 | No | No | Current |